ID: ALA5267586

Max Phase: Preclinical

Molecular Formula: C35H34O8

Molecular Weight: 582.65

Associated Items:

Representations

Canonical SMILES:  COc1cc(O)c([C@H](/C=C/C[C@@H](O)CCc2ccc(O)cc2)c2ccc(O)cc2)c(O)c1C(=O)/C=C/c1ccc(O)cc1

Standard InChI:  InChI=1S/C35H34O8/c1-43-32-21-31(41)33(35(42)34(32)30(40)20-10-23-8-16-27(38)17-9-23)29(24-11-18-28(39)19-12-24)4-2-3-25(36)13-5-22-6-14-26(37)15-7-22/h2,4,6-12,14-21,25,29,36-39,41-42H,3,5,13H2,1H3/b4-2+,20-10+/t25-,29-/m1/s1

Standard InChI Key:  DHYXVFFHVYUZJU-IQCVCLICSA-N

Associated Targets(non-human)

J774.1 238 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 582.65Molecular Weight (Monoisotopic): 582.2254AlogP: 6.19#Rotatable Bonds: 12
Polar Surface Area: 147.68Molecular Species: NEUTRALHBA: 8HBD: 6
#RO5 Violations: 3HBA (Lipinski): 8HBD (Lipinski): 6#RO5 Violations (Lipinski): 3
CX Acidic pKa: 6.94CX Basic pKa: CX LogP: 7.30CX LogD: 6.69
Aromatic Rings: 4Heavy Atoms: 43QED Weighted: 0.07Np Likeness Score: 1.26

References

1. Vanucci-Bacqué C, Bedos-Belval F..  (2021)  Anti-inflammatory activity of naturally occuring diarylheptanoids - A review.,  31  [PMID:33422907] [10.1016/j.bmc.2020.115971]

Source